Dear customers,

we have started to provide the documents for our products in an electronic format. These are the Instructions for Use (IFU), the Safety Data Sheets (SDS) and the Certificate of Analysis (CoA). For batches placed on the market after 01 January 2023, you can find our documents on the eIFU portal https://eifu.r-biopharm.com.

RIDA®GENE MRSA

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Verwendungszweck:Für die in-vitro Diagnostik. Der RIDA®GENE MRSA Test, der auf dem Roche LightCycler® 480 II durchgeführt wird, ist eine multiplex real-time PCR zum direkten qualitativen Nachweis [...]